Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies

被引:25
作者
Ahmad, Ashfaq [1 ]
Ullah, Farhat [1 ]
Sadiq, Abdul [1 ]
Ayaz, Muhammad [1 ]
Rahim, Haroon [2 ]
Rashid, Umer [3 ]
Ahmad, Sajjad [1 ]
Jan, Muhammad Saeed [1 ]
Ullah, Riaz [4 ]
Shahat, Abdelaaty A. [4 ,5 ]
Mahmood, Hafiz Majid [6 ]
机构
[1] Univ Malakand, Dept Pharm, Dir L 18000, KP, Pakistan
[2] Sarhad Univ Sci & Informat Technol, Dept Pharm, Peshawar, KP, Pakistan
[3] COMSATS Univ Islamabad, Dept Chem, Abbottabad Campus, Abbottabad 22060, KP, Pakistan
[4] King Saud Univ Riyadh, Coll Pharm, Dept Pharmacognosy MAPPRC, Riyadh, Saudi Arabia
[5] Natl Res Ctr, Phytochem Dept, Giza, Egypt
[6] King Saud Univ, Coll Pharm, Dept Pharmacol, Riyadh 11451, Saudi Arabia
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2019年 / 13卷
关键词
Succinimide; Alzheimer's disease; MTT; oxidative stress; diabetes; helminthiasis;
D O I
10.2147/DDDT.S226080
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Purpose: The current work was designed to synthesize a bioactive derivative of succinimide and evaluate it for anti-Alzheimer, anticancer and anti-diabetic potentials. Methods: The compound was synthesized by Michael addition of butyraldehyde with N-phenylmaleimide. The synthesized compound was screened for biological potentials including anti-cholinesterase, in-vitro anti-diabetic, antioxidant and anthelmintic potentials. The anti-cholinesterase potential was evaluated against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), anti-diabetic potential against alpha-glucosidase, antioxidant potential against ABTS, DPPH and H2O2 and anthelmintic potential against Perethima posthuma and Ascaridia galli respectively. Results: The compound demonstrated significant AChE and BChE inhibition i.e., 71.34 +/- 1.92 and 73.42 +/- 1.92 at the concentration of 1000 mu g/mL respectively. Other dilutions exhibited concentration-dependent inhibitory activity against both enzymes. In the MTT assay, the newly synthesized compound was found active against all of the cell lines viz, HCT-116, MDA-MB231, NIH/3T3 and MCF-7 and the highest cytotoxicity potential was observed against the colon cancer cell line (HCT-116) with an IC50 value of 78 mu g/mL exhibiting its highest potential. Moreover, the compound exhibited prominent alpha-glucosidase inhibitory potentials (79.86 +/- 2.54% at 1000 mu g/mL) with IC50 value of 156.23 mu g/mL. Further, our test compound exhibited considerable scavenging activity against DPPH, ABTS and H-2 O-2 free radicals with percent inhibitions of 75.84 +/- 1.58, 72.85 +/- 1.17 and 54.82 +/- 1.82 and IC50 values of 84.36, 139.74 and 752.21 mu g/mL respectively. Our test sample exhibited significant anthelmintic potentials. It demonstrated significant paralysis and death of the test worms in an unbelievably short time in comparison with albendazole. Conclusion: Going into the detail of all observations, it may be deduced that the newly synthesized succinimide derivative could be an important drug candidate against neurodegenerative disorders like Alzheimer's disease, cancer, diabetes mellitus and worms. Further detailed studies in animal models are required for in-vivo analysis of the compound.
引用
收藏
页码:4185 / 4194
页数:10
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